Process for the production of 5-(4-((2s,5s)-5-(4-chlorobenzyl)-2-methyl-morpholino)piperidin-1-yl)-1h-1,2,4-triazol-3-amine

ABSTRACT

The present invention relates to a process for the synthesis of 5-(4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)piperidin-1-yl)-1H-1,2,4-triazol-3-amine in two hydrated crystalline forms and in one anhydrous crystalline form. The present invention further relates to methyl (Z)-4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)-N-cyanopiperidine-1-carbimidothioate which is an intermediate in this process.

RELATED APPLICATIONS

This application claims the benefit of priority to Polish Patent Application number P.431269, filed Sep. 25, 2019; and U.S. Provisional Patent Application Ser. No. 62/905,494, filed Sep. 25, 2019.

FIELD OF INVENTION

The present invention relates to a process for the synthesis of 5-(4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)piperidin-1-yl)-1H-1,2,4-triazol-3-amine in two hydrated and one anhydrous crystalline forms. The present invention further relates to methyl (Z)-4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)-N-cyanopiperidine-1-carbimidothioate which is an intermediate in this process.

BACKGROUND OF THE INVENTION

5-(4-((2S,5S)-5-(4-Chlorobenzyl)-2-methylmorpholino)piperidin-1-yl)-1H-1,2,4-triazol-3-amine of structural formula 1 has been first described in international patent application WO 2017/037670 (incorporated by reference).

The compound of formula 1 is a dual inhibitor of Acidic Mammal Chitinase (AMCase) and Chitotriosidase 1 (CHIT-1). Such compounds might be used in a treatment of disorders associated with an overexpression of those enzymes. Such disorders are asthma and allergic responses or idiopathic pulmonary fibrosis (IPF) and chronic obstructive pulmonary disease (COPD).

The patent application WO 2017/037670 describes a synthesis of the compound of formula 1 from (2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholine of formula 2. This synthesis is outlined in the scheme below.

The compound of formula 2 is reacted with N-(tert-butoxycarbonyl)-4-piperidone of formula 3, sodium triacetoxyborohydride as a reducing agent and glacial acetic acid in 1,2-dichloroethane. After a night crude tert-butyl 4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)-piperidine-1-carboxylate of formula 4 is isolated by extraction and purified by column chromatography. The pure compound of formula 4 is subjected to a reaction of deprotection of tert-butoxycarbonyl moiety by solution of hydrogen chloride in ethyl acetate resulting in (2S,5S)-5-(4-chlorobenzyl)-2-methyl-4-(piperidin-4-yl)morpholine of formula 5 as a dihydrochloride. In the next step, the compound of formula 5 is reacted with dimethyl N-cyanodithioiminocarbonate in the presence of potassium carbonate as a base in acetonitrile. After few hours of heating, hydrazine monohydrate is added and the reaction mixture is further refluxed for few hours. When the suspension reaches ambient temperature, the solid material is filtered off and the crude product obtained by concentration of the filtrate is purified by column chromatography on silica gel followed by precipitation, yielding the compound of formula 1.

The conversion of the compound of formula 5 into the compound of formula 1 is a sequence of two reactions. In the first step, the compound of formula 5 is converted into an intermediate which is most likely (Z)-4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)-N-cyanopiperidine-1-carbimidothioate of formula 6.

The synthesis of the compound of formula 1 as described in the patent application WO 2017/037670 requires two chromatographic purifications, which are cost-ineffective and time consuming. The process involving chromatographic purification rather cannot be considered suitable for industrial scaling up. There is no information if the material obtained in the process is obtained in a crystalline form, which might be considered as stable. Moreover, the Particles Size Distribution is an important parameter of a drug substance, which might have a big impact on the production of drug product in a form of tablets. The patent does not teach if the simple precipitation of the final product as described leads to a material with strictly defined particles size in a repeatable manner. Since the last step of the synthesis presented in WO 2017/037670 requires use of hydrazine, which is known for its carcinogenic properties, the level of the residual hydrazine in the drug substance must be strictly controlled besides of the total purity of the material which is a key factor of every process in the synthesis of a drug substance. According to the features outlined above, there is unmet need for the scalable and efficient process for the synthesis of 5-(4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)-piperidin-1-yl)-1H-1,2,4-triazol-3-amine of formula 1 which is suitable for the production of a drug product.

SUMMARY OF THE INVENTION

The present invention provides a process for the synthesis of (2S,5S)-5-(4-chlorobenzyl)-2-methyl-4-(piperidin-4-yl)morpholine of formula 5 dihydrochloride hydrate in a solid crystalline state.

The present invention relates to methyl (Z)-4-((2S,5S)-5-(4-chlorobenzyl)-2-methyl-morpholino)-N-cyanopiperidine-1-carbimidothioate of formula 6 in a solid crystalline state characterized by at least one of below:

-   -   (i) XRPD peaks at 10.13, 10.98, 12.03, 13.54, 13.98, 14.40,         14.88, 16.84, 18.67, 20.21, 20.85, 21.71, 22.56, 22.98, 24.10,         24.56, 25.27, 27.48, 29.80, 30.43, and 33.36° 2-theta.     -   (ii) IR bands at 2959, 2926, 2866, 2820, 2795, 2167, 1541, 1491,         1450, 1431, 1383, 1358, 1273, 1215, 1151, 1117, 1096, 1070,         1043, 1013, 988, 930, 862, 833, 806, 714, 665, and 638 cm′.     -   (iii) DSC onset at 156.26° C. and a peak at 157.51° C.

The aforementioned characteristics are substantially in accordance with FIGS. 2 to 4.

The present invention provides a process for the synthesis of methyl (Z)-4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)-N-cyanopiperidine-1-carbimidothioate of formula 6 in a solid crystalline state.

The present invention further relates to 5-(4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)piperidin-1-yl)-1H-1,2,4-triazol-3-amine of formula 1 hydrated form I in a solid crystalline state characterized by at least one of below:

-   -   (i) XRPD peaks at 6.70, 9.96, 10.68, 12.74, 13.42, 14.20, 14.82,         15.40, 15.58, 16.44, 17.00, 17.46, 18.02, 18.30, 18.64, 19.52,         20.16, 20.66, 21.40, 21.64, 21.86, 22.16, 22.58, 23.22, 23.68,         24.64, 27.00, 27.26, 27.88, and 28.84° 2-theta.     -   (ii) IR bands at 3318, 3206, 2963, 2934, 2859, 2833, 1636, 1589,         1553, 1489, 1462, 1404, 1346, 1314, 1277, 1250, 1151, 117, 1092,         1069, 1013, 917, 868, 829, 800, 764, 725, and 673 cm⁻¹.     -   (iii) DSC onset at 80.60° C. and a peak at 91.32° C.

The aforementioned characteristics are substantially in accordance with FIGS. 7 to 9.

The present invention provides a process for the synthesis of 5-(4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)piperidin-1-yl)-1H-1,2,4-triazol-3-amine of formula 1 hydrated form I in a solid crystalline state.

The present invention further relates to 5-(4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)piperidin-1-yl)-1H-1,2,4-triazol-3-amine of formula 1 anhydrous form in a solid crystalline state characterized by at least one of below:

-   -   (i) XRPD peaks at 5.81, 7.39, 9.95, 11.53, 11.97, 12.39, 13.13,         14.07, 14.60, 14.81, 15.11, 16.09, 16.45, 17.15, 17.67, 17.85,         18.21, 18.68, 19.21, 19.84, 20.75, 21.22, 22.24, 23.00, 24.22,         24.98, and 27.48° 2-theta.     -   (ii) IR bands at 3252, 3198, 3119, 2955, 2924, 2857, 2793, 1666,         1599, 1543, 1483, 1456, 1404, 1337, 1283, 1248, 1136, 1117,         1094, 1072, 1053, 1013, 908, 858, 795, and 718 cm⁻¹.     -   (iii) DSC onset at 175.83° C. and a peak at 177.59° C.

The aforementioned characteristics are substantially in accordance with FIGS. 10 to 12.

The present invention further provides a preparation of 5-(4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)piperidin-1-yl)-1H-1,2,4-triazol-3-amine of formula 1 anhydrous form in a solid crystalline state.

The present invention further relates to 5-(4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)piperidin-1-yl)-1H-1,2,4-triazol-3-amine of formula 1 hydrated form II in a solid crystalline state characterized by at least one of below:

-   -   (i) XRPD peaks at 10.14, 12.88, 13.50, 13.94, 15.30, 15.48,         16.12, 16.34, 17.60, 17.98, 18.14, 18.64, 18.72, 19.34, 19.76,         20.16, 20.36, 21.64, 22.16, 22.54, 22.86, 23.02, 23.70, 24.28,         25.92, 26.14, 26.32, 27.08, 27.34, 27.70, 30.50, and 39.24°         2-theta.     -   (ii) IR bands at 3325, 2963, 2814, 1634, 1580, 1553, 1489, 1460,         1418, 1389, 1343, 1279, 1248, 1206, 1151, 1119, 1090, 1069,         1047, 1013, 991, 914, 866, 831, 797, 760, 665, and 600 cm⁻¹.     -   (iii) Two DSC peaks: first with onset at 60.12° C. and a peak at         70.29° C. Second with onset at 82.83° C. and a peak at 90.87° C.

The aforementioned characteristics are substantially in accordance with FIGS. 15 to 17.

The present invention provides a process for the synthesis of 5-(4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)piperidin-1-yl)-1H-1,2,4-triazol-3-amine of formula 1 hydrated form II in a solid crystalline state.

The present invention further relates to 5-(4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)piperidin-1-yl)-1H-1,2,4-triazol-3-amine of formula 1 amorphous form in a solid state characterized by:

-   -   (i) IR bands at 3312, 3173, 2968, 2859, 2822, 1634, 1551, 1489,         1458, 1346, 1277, 1246, 1150, 1115, 1094, 1069, 1013, 920, 858,         804, 758, 719, and 665 cm⁻¹.

The aforementioned characteristic is substantially in accordance with FIG. 18.

The present invention provides a method for the preparation of 5-(4-((2S,5S)-5-(4-chloro-benzyl)-2-methylmorpholino)piperidin-1-yl)-1H-1,2,4-triazol-3-amine of formula 1 amorphous form in a solid state.

The present invention provides industrially scalable methods for the synthesis of the compound of formula 1. The methods avoid chromatographic purifications, which were the most tedious parts of the process. The final product is obtained in a repeatable manner in terms of particle size distribution, purity and the residual hydrazine level, and meets high standards for drug substances.

BRIEF DESCRIPTION OF DRAWINGS

FIG. 1. Scheme of the synthesis of various forms of 5-(4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)piperidin-1-yl)-1H-1,2,4-triazol-3-amine.

FIG. 2. XPRD diffractogram of methyl (Z)-4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)-N-cyanopiperidine-1-carbimidothioate obtained in Example 3.

FIG. 3. FT-IR (ATR) spectrum of methyl (Z)-4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)-N-cyanopiperidine-1-carbimidothioate obtained in Example 3.

FIG. 4. DSC thermogram of methyl (Z)-4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)-N-cyanopiperidine-1-carbimidothioate obtained in Example 3.

FIG. 5. ¹H NMR spectrum (CDCl₃ at 400 MHz) of methyl (Z)-4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)-N-cyanopiperidine-1-carbimidothioate obtained in Example 3.

FIG. 6. ¹³C NMR spectrum (CDCl₃ at 100 MHz) of methyl (Z)-4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)-N-cyanopiperidine-1-carbimidothioate obtained in Example 3.

FIG. 7. XPRD diffractogram of 5-(4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)piperidin-1-yl)-1H-1,2,4-triazol-3-amine hydrated form I calculated from X-ray analysis of a single crystal obtained from a mixture of water and ethanol.

FIG. 8. FT-IR (ATR) spectrum of 5-(4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)piperidin-1-yl)-1H-1,2,4-triazol-3-amine hydrated form I obtained in Example 6.

FIG. 9. DSC thermogram of 5-(4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)piperidin-1-yl)-1H-1,2,4-triazol-3-amine hydrated form I obtained in Example 6.

FIG. 10. XPRD diffractogram of 5-(4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)piperidin-1-yl)-1H-1,2,4-triazol-3-amine anhydrous form obtained in Example 8.

FIG. 11. FT-IR (ATR) spectrum of 5-(4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)piperidin-1-yl)-1H-1,2,4-triazol-3-amine anhydrous form obtained in Example 8.

FIG. 12. DSC thermogram of 5-(4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)piperidin-1-yl)-1H-1,2,4-triazol-3-amine anhydrous form obtained in Example 8.

FIG. 13. ¹H NMR (C₆D₆ at 700 MHz) spectrum of 5-(4-((2S,5S)-5-(4-chlorobenzyl)-2-methyl-morpho-lino)piperidin-1-yl)-1H-1,2,4-triazol-3-amine anhydrous form obtained in Example 8.

FIG. 14. ¹³C NMR (C₆D₆ at 176 MHz) spectrum of 5-(4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)piperidin-1-yl)-1H-1,2,4-triazol-3-amine anhydrous form obtained in Example 8.

FIG. 15. XPRD diffractogram of 5-(4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)piperidin-1-yl)-1H-1,2,4-triazol-3-amine hydrated form II calculated from X-ray analysis of a single crystal obtained from a mixture of water and methanol.

FIG. 16. FT-IR (ATR) spectrum of 5-(4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)piperidin-1-yl)-1H-1,2,4-triazol-3-amine hydrated form II obtained in Example 10.

FIG. 17. DSC thermogram of 5-(4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)piperidin-1-yl)-1H-1,2,4-triazol-3-amine hydrated form II form obtained in Example 10.

FIG. 18. FT-IR (ATR) spectrum of 5-(4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)piperidin-1-yl)-1H-1,2,4-triazol-3-amine amorphous form obtained in Example 11.

DETAILED DESCRIPTION OF THE INVENTION

The present invention provides the efficient and scalable process for the synthesis of (2S,5S)-5-(4-chlorobenzyl)-2-methyl-4-(piperidin-4-yl)morpholine of formula 5. Compared to the description of the original approach outlined in the “Background of the Invention”, various changes were introduced into the procedure in order to improve yield and simplify the synthesis, making it scalable. The compound of formula 2 is reacted with N-(tert-butoxycarbonyl)-4-piperidone of formula 3, in the presence of a reducing agent, sodium cyanoborohydride and an additive, preferably zinc chloride in a solvent, preferably an alcohol, more preferably in methanol, at a temperature from 0° C. to reflux, preferably at ambient temperature. When full conversion of the starting material is obtained, tert-butyl 4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)piperidine-1-carboxylate of formula 4 is isolated by extraction and the crude product is dissolved in a solvent, preferably ethyl acetate, and a solution of hydrochloric acid, preferably concentrated hydrochloric acid, is added. When full conversion of the starting material is obtained, the solvent is swapped to a polar solvent, preferably to methanol. To the solution a solvent, preferably acetone, is added and the solution is allowed to cool down to ambient temperature. The product crystallizes upon cooling and the crystals are filtered off. The filter cake is rinsed with a solvent, preferably acetone, and dried in the air to afford (2S,5S)-5-(4-chlorobenzyl)-2-methyl-4-(piperidin-4-yl)morpholine of formula 5 as white crystals. Careful analysis of the obtained material showed that the product was obtained as dihydrochloride hydrate.

A crucial step in the synthesis of the compound formula 2 is the reaction of a mixture of the compounds of formula 7 and 8 with potassium tert-butoxide leading to an amide of formula 9. Only the compound of formula 8 cyclizes into the compound of formula 9. In the reaction conditions, the compound of formula 7 epimerizes into the compound of formula 8 which cyclizes into the compound of formula 9. Due to that fact, the reaction of potassium tert-butoxide with the mixture of the compounds of formula 7 and 8 provides exclusively the compound of formula 9. The compound of formula 9 epimerizes in the reaction conditions to a compound of formula 10 which is a by-product of the reaction. The crude product of formula 9 is then crystallized but complete removal of the unwanted compound of formula 10 is tedious and leads to significant loss of the product. Reduction of the compound of formula 9 leads to the compound of formula 2, but when the compound of formula 9 is contaminated with the compound of the formula 10, then the compound of formula 2 contains the compound of formula 11 obtained as the product of reduction of the compound of formula 10.

Under conditions described in the patent application WO 2017/037670 (sodium triacetoxyborohydride, acetic acid and 1,2-dichloroethane), the compound of formula 11 reacts with N-Boc-4-piperidinone leading to a by-product of formula 12 which is observed in crude compound of formula 3. The impurity of formula 12 can be removed by the careful purification on silica gel but such an approach is unacceptable on a kilo-scale. The compound of formula 11 does not react with N-Boc-4-piperidinone when conditions described in this patent application (sodium cyanoborohydride, zinc chloride and methanol) are used. Since the compound of formula 11 can be easily removed by crystallization after removal of the tert-butoxycarbonyl protection group, the present invention relates to a method for the synthesis of the compound of formula 5 with no impurity of formula 13. Moreover, the conditions described in this application unobviously allow one to use hydrochloride salt of the compound of formula 2 as the starting material which can facilitate the process. The compound of formula 2 is an oil of limited stability, what means that it must be kept in a form of salt in order to prevent decomposition. To the contrary, the reaction described in WO 2017/037670 is not proceeding when hydrochloride of the compound of formula 2 is used as the starting material and the salt must be first converted into the free base which is an additional operation.

The present invention further provides a method for the synthesis of methyl (Z)-4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)-N-cyanopiperidine-1-carbimidothioate of formula 6. This compound was never isolated nor described yet. The related compound can be synthetized by the reaction of (2S,5S)-5-(4-chlorobenzyl)-2-methyl-4-(piperidin-4-yl)morpholine of formula 5 with dimethyl N-cyanodithioiminocarbonate in the presence of a base, preferably trialkylamine, more preferably triethylamine, in a solvent, preferably ethanol, 1-propanol or 2-propanol. The reaction is carried out at a temperature from room temperature to reflux, preferably at 50° C. The reaction mixture is allowed to cool down to ambient temperature when full conversion of the starting material is obtained. The product crystallizes upon cooling. The material is filtered off and the filter cake is washed with the solvent, preferably ethanol, 1-propanol, or 2-propanol, and dried to afford the compound of formula 6.

The present invention further provides a method for the synthesis of the compound of formula 6 directly from the compound of formula 2 avoiding the three-step synthesis. This approach relates to the reaction of the compound of formula 2 with 4-oxopiperidine methyl N-cyanothioimidocarbamate of formula 14. The compound of formula 14 can be easily obtained from commercially available 4,4-dihydroxypiperidine hydrochloride by a reaction with dimethyl N-cyanodithioiminocarbonate in the presence of a base, preferably trialkylamine, more preferably triethylamine, in a solvent, preferably in a mixture of solvents, and more preferably in a mixture of 2-propanol and water, at a temperature from 0 ρC to reflux, preferably at ambient temperature. The reaction mixture is quenched with 6 M solution of hydrochloric acid and extracted with organic solvent, preferably dichloromethane. The solution is washed with water and the solvent is swapped to a polar solvent, preferably 2-propanol. To the hot solution, a non-polar solvent, preferably isopropyl ether, is added, leading to crystallization of the product. The solid is filtered off and the filter cake is rinsed with a solvent, preferably with a mixture of solvents, and more preferably with a mixture of 2-propanol and isopropyl ether, and then dried to afford the compound of formula 14 as an off-white solid.

The reaction between the compound of formula 2 and the compound of formula 14 carried out in the conditions described in WO 217/037670 for the synthesis the compound of the formula 4 did not proceed after simple replacing the ketone compound of formula 3 with the ketone compound of formula 14. Moreover, the conditions for the synthesis of the compound of formula 4 from the compound of formula 2, as described in this application, led to a mixture of the compound of formula 6 and a by-product of formula 15, after simple replacing the compound of formula 3 with the compound of formula 14. This gave rise to an unmet need to develop new conditions for the synthesis of the compound of formula 6 directly from the compound of the formula 2.

The reaction between the compound of formula 2 and the compound of formula 14 is carried out in the presence of a reducing agent, preferably sodium cyanoborohydride, and an additive, preferably zinc chloride, in a polar solvent, preferably ethanol, at a temperature from 0° C. to reflux, preferably at ambient temperature. After full conversion of the starting material is obtained, the reaction mixture is quenched with a 1 M solution of sodium hydroxide and extracted with organic solvent, preferably dichloromethane. The solvent is swapped to organic solvent, preferably ethanol. The solution is allowed to cool down to ambient temperature, leading to crystallization of the product. The solid is filtered off and the filter cake is rinsed with a solvent, preferably with ethanol, and dried to afford the compound of formula 6 as a white solid.

The target molecule of formula 1 can be obtained either from the compound of formula 5 or the compound of formula 6. Moreover, this patent application describes methods for the preparation of an anhydrous form, two hydrated forms (hydrated forms I and II) and an amorphous form of the target molecule of formula 1. The methods outlined in this paragraph are summarized in FIG. 1.

The present invention further provides a method for the synthesis of the compound of formula 1 hydrated form I from the compound of formula 5 (reaction A in FIG. 1). The compound of formula 5 is suspended in a solvent, preferably in ethanol, and dimethyl N-cyanodithioiminocarbonate is added, followed by a base, preferably trialkylamine, more preferably triethylamine, at a temperature from ambient temperature to boiling point, preferably at 40° C. When full conversion of the starting material is achieved, hydrazine monohydrate is added, the reaction is continued at a temperature from ambient temperature to boiling point, preferably at 60° C. When full conversion of the intermediate is achieved, water is added, and the solution is cooled down to a temperature from −20° C. to ambient temperature, preferably to 5° C. The precipitated solid is filtered off and the filter cake is rinsed with a mixture of water and an organic solvent, preferably ethanol, and dried to afford the compound of formula 1 hydrated form I as a white solid.

The present invention further provides method for the synthesis of the compound of formula 1 hydrated form I from the compound of formula 6 (reaction B in FIG. 1). The compound of formula 6 is suspended in a solvent, preferably in ethanol, at a temperature from ambient temperature to boiling point, preferably at 60° C., and hydrazine monohydrate is added. When full conversion of the starting material is achieved, water is added and the solution is cooled down to a temperature from −20° C. to ambient temperature, preferably to 5° C. The precipitated solid is filtered off and the filter cake is rinsed with a mixture of water and an organic solvent, preferably ethanol, and dried to afford the compound of formula 1 hydrated form I as a white solid.

The present invention further provides a method for the synthesis of the compound of formula 1 anhydrous form from the compound of formula 6 (reaction C in FIG. 1). The reaction of the compound of formula 6 with hydrazine monohydrate is carried out in an organic solvent, preferably acetonitrile, at a temperature from ambient temperature to boiling point, preferably at 60° C. When full conversion of the starting material is achieved, the solution is allowed to cool down to ambient temperature and the product precipitates upon cooling. The solid is filtered off and the filter cake is rinsed with a solvent, preferably with acetonitrile, and dried to afford the compound of formula 1 anhydrous form as a white solid.

Compared to WO 2017/037670, when the compound of the formula 1 was obtained in a one-pot approach, the process employing separation of the compound of the formula 6 unobviously allows to obtain the compound of the formula 1 anhydrous form in higher yield (86% in this application versus 72% in WO 2017/037670). The crucial factor of the second step involving reaction of the compound of formula 6 is acetonitrile used as the solvent. In more polar solvents (i.e., methanol, ethanol or 2-propanol), yield of the reaction is much lower. On the other hand, when less polar solvents (i.e., dichloromethane, methyl tert-butyl ether or toluene) are applied, the level of residual hydrazine becomes unacceptable.

The present invention further provides a method for the preparation of the anhydrous form of the compound of formula 1 from its hydrated form I (method D in FIG. 1). The compound of formula 1 in hydrated form I is suspended in an organic solvent, preferably in ethyl acetate, and the suspension is heated up to reflux. Upon heating the suspension turns into a clear solution. The solution is distilled until the temperature of volatiles reaches 76° C. During distillation the product precipitates. The solid is filtered off at ambient temperature. The filter cake is rinsed with an organic solvent, preferably ethyl acetate, and dried to afford the compound of formula 1 in the anhydrous form as white crystals.

The synthesis of the compound of formula 1 hydrated form I followed by the synthesis of the compound of the formula 1 anhydrous form has a significant advantage as compared to the synthesis of the compound of formula 1 described in WO 2017/037670. Under new conditions, the precipitation of the compound of the formula 1 hydrated form I unobviously allows to control the amount of residual hydrazine which is considered as a genotoxic impurity and must be controlled at ppm levels. The method outlined in the previous paragraph was used for the synthesis of three batches of the anhydrous form of the compound of formula 1. This material was carefully analyzed for purity, residual hydrazine level and particle size distribution.

Purity Residual hydrazine Particle size by HPLC level distribution 99.92% 0.3 ppm D10 152 μm, D50 255 μm, D90 403 μm ≥99.95% 0.1 ppm D10 202 μm, D50 357 μm, D90 577 μm ≥99.95% 0.2 ppm D10 154 μm, D50 284 μm, D90 485 μm

The present invention further provides a method for the preparation of the hydrated form II of the compound of formula 1 from its anhydrous form (method E in FIG. 1). The compound of the formula 1 anhydrous form is dissolved in methanol at reflux. To the solution water is added and product precipitates. The suspension is allowed to cool down to a temperature from −20° C. to ambient temperature, preferably to 5° C. The solid as aged and filtered off. The filter cake is rinsed with a mixture of water and methanol, and dried to afford the compound of formula 1 hydrated form II as a white solid.

Due to the fact that the compound of formula 6 is not stable in methanol, it is not possible to obtain the hydrated form II directly from the compound 6 as for hydrated form I of the compound of formula 1. Both hydrated forms I and II of the compound of formula 1 are unstable, leading to amorphous form upon drying. The XPRD data for the dried material and data calculated from X-ray structure differ. Moreover, analysis of a dried single crystal of the compound of formula 1 hydrated form I used from structure determination showed lack of crystalline structure which leads to a conclusion that crystal structure collapses upon drying. The amorphous form of the compound of formula 1 can be prepared in a more convenient way by melting the anhydrous form or hydrated form I or II of the compound of formula 1 followed by cooling off the material to ambient temperature. After grinding the glass-like solid, anhydrous form of the compound of formula 1 is an off-white solid.

EXAMPLES

The invention will be illustrated by the following examples.

The following examples are provided for illustrative purposes only and are not intended to limit the scope of the invention in any way.

General Procedures

All solvents, substrates and reagents that were commercially available were used without further purification.

NMR spectra were recorded on Agilent Mercury 400 MHz spectrometer and Bruker Avance 500, and 700 MHz spectrometers (DXR500, and DXR700, respectively).

NMR spectra were recorded in the indicated deuterated solvents that were commercially available.

Resonances are given in parts per million relative to tetramethylsilane (δ 0.00 ppm for CD₃Cl) or residual solvent (δ 4.87 ppm for CD₃OD or δ 7.61 ppm for C₆D₆) for ¹H NMR, or to solvent (δ 49.00 ppm for CD₃OD, δ 77.26 ppm for CDCl₃ or δ 128.06 ppm for C₆D₆) for ¹³C NMR). Data are reported as follows: chemical shift (δ), multiplicity (s=singlet, d=doublet, t=triplet, m=multiplet, bs=broad singlet), coupling constants (J in Hz) and integration.

FT-IR spectra were recorded with Shimadzu IRTracer-100 in ATR mode (zinc selenide crystal).

X-ray diffraction experiments at T=100(2) K were performed on good-quality single crystals. The crystals were mounted with Paratone-N oil to the MiTeGen micromount. Diffraction data were collected on the Agilent Technologies SuperNova Dual Source with the CuKα radiation (λ=1.54184 Å). The lattice parameters were obtained by least-squares fit to the optimized setting angles of the reflections collected by using the CrysAlis CCD software. Data were reduced using the CrysAlis RED program. The multi-scan empirical absorption correction using spherical harmonics, implemented in SCALE3 ABSPACK scaling algorithm, was applied. The structural determination procedure was carried out using the SHELX package.

XPRD diffractograms of compounds obtained in Examples 3 and 8 were recorded with Bruker D8 Discover powder X-ray diffractometer equipped with Cu CuKα radiation (1.54 Å) and Vantec detector. The samples were analyzed in a continuous mode with step size of 0.01222276° and step time of 0.9 s over an angular range of 3-50° 2θ. XPRD diffractograms of compounds obtained in Examples 6 and 10 were calculated from single-crystal X-ray data using Mercury software.

DSC thermograms were recorded with Mettler Toledo DSC 3 at 5° C./min. gradient.

PSD data were recoded with Malvern Mastersizer 2000 in Isopar G.

The purity was measured by HPLC-UV method. The analysis is performed on Phenyl-Hexyl analytical column (Kinetex Phenyl-Hexyl, 2.1 mm×100 mm; 2.6 μm) at 20° C., and at mobile phase flow rate of 0.3 mL/min. The mobile phase is a mixture of solvent A (900 mL water, 100 mL methanol, 1 g ammonium formate) and solvent B (100 mL water, 900 mL methanol, 1 g ammonium formate). Elution is carried out under gradient elution (60% of solvent B from 0.0 to 2.0 min then from 60% to 85% of solvent B from 2.0 to 2.5 min then 85% of solvent B from 2.5 to 5.5 min then from 85% to 100% of solvent B from 5.5 to 6.0 min then 100% of solvent B from 6.0 to 8.0 min then from 100% to 60% of solvent B from 8.0 to 8.2 min then at 60% of solvent B from 8.2 to 13.0 min). Peaks are recorded using UV detection at 225 nm.

The residual level of hydrazine was measured by HPLC-UV method. A sample is prepared by dissolution of 75 mg in 1 mL of methanol. 1 mL of 1 M HCl solution is added followed by 1 mL of benzaldehyde solution (0.6 g/mL in methanol/water 1/1 (v/v)) and the solution is vortexed. 1 mL of n-heptane is added and the biphasic system is vortexed and centrifuged at high speed. The upper phase (5 μL) is injected for analysis. Chromatographic (HPLC-UV) analysis is performed on C18 analytical column (LumiSep C18, 2.1 mm×50 mm; 3 μm) maintained at 40° C., and mobile phase flow rate of 0.5 mL/min. The mobile phase is composed of a mixture of solvent A (900 mL water, 100 mL acetonitrile, 1 g ammonium formate) and solvent B (100 mL water, 900 mL acetonitrile, 1 g ammonium formate). Elution is carried out under isocratic conditions (55% of solvent B until completion of the run at 6 min.) Peaks are recorded using UV detection at 305 nm. Benzaldehyde hydrazone retention time is ca. 2.43 min.

Boc denotes tert-butoxycarbonyl protecting group.

Reaction yields are expressed by mole %.

HPLC purities are expressed by area-under-the-curve %.

Content of water by Karl Fischer method and loss on drying are expressed by weight %.

Example 1 Preparation of (2S,5S)-5-(4-chlorobenzyl)-2-methyl-4-(piperidin-4-yl)morpholine dihydrochloride hydrate (4, dihydrochloride hydrate) from (2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholine (2)

(2S,5S)-5-(4-Chlorobenzyl)-2-methylmorpholine (2, 13.06 g), N-Boc-4-piperidinone (3, 17.30 g) and zinc chloride (7.89 g) were dissolved in methanol (130 mL). Sodium cyanoborohydride (5.45 g) was added portionwise and the reaction was stirred overnight. The reaction mixture was partitioned between ethyl acetate (240 mL) and 1 M sodium hydroxide solution (240 mL). The aqueous layer was extracted with ethyl acetate (240 mL), and the combined extracts were washed with half-saturated sodium chloride solution (240 mL), and dried. The solution was concentrated to ca. 200 mL and concentrated hydrochloric acid (40 mL) was added. After half an hour water was distilled off using a Dean-Stark trap. Ethyl acetate was swapped for methanol and concentrated to ca. 100 mL of volume. To the solution, acetone (300 mL) was slowly added leading to precipitation of the product. The suspension was allowed to cool down to ambient temperature and aged for an hour. The solid was filtered off and the filter cake was rinsed with acetone (2×100 mL) and dried in the air to afford (2S,5S)-5-(4-chloro-benzyl)-2-methyl-4-(piperidin-4-yl)morpholine dihydrochloride hydrate (4, dihydrochloride hydrate, 20.92 g, 90% yield over two steps, 99.5% purity by HPLC) as a white solid.

¹H NMR (500 MHz, CD₃OD) δ 7.40-7.30 (m, 4H), 4.08-3.98 (m, 1H), 3.96-3.83 (m, 2H), 3.82-3.74 (m, 1H), 3.69 (d, J=13.3 Hz, 1H), 3.67-3.54 (m, 3H), 3.29-3.06 (m, 5H), 2.60-2.50 (m, 2H), 2.26-2.11 (m, 2H), and 1.32 (d, J=6.2 Hz, 3H) ppm.

¹³C NMR (125 MHz, CD₃OD) δ 135.2, 134.4, 132.5, 130.1, 71.7, 65.7, 58.0, 57.6, 50.4, 43.7, 43.5, 28.4, 25.2, 25.0, and 18.7 ppm.

Example 2 Preparation of (2S,5S)-5-(4-chlorobenzyl)-2-methyl-4-(piperidin-4-yl)morpholine dihydrochloride hydrate (4, dihydrochloride hydrate) from (2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholine hydrochloride (2, hydrochloride)

(2S,5S)-5-(4-Chlorobenzyl)-2-methylmorpholine (2, hydrochloride, 9.99 g), N-Boc-4-piperidinone (3, 11.39 g) and zinc chloride (5.23 g) were dissolved in methanol (80 mL). Sodium cyanoborohydride (3.71 g) was added portionwise and the reaction was stirred overnight. The reaction mixture was partitioned between ethyl acetate (240 mL) and 1 M sodium hydroxide solution (240 mL). The aqueous layer was extracted with ethyl acetate (240 mL), and the combined extracts were washed with half-saturated sodium chloride solution (240 mL), and dried. The solution was concentrated to dryness and the residue was dissolved in 3 M hydrochloric acid solution in ethyl acetate. After an hour the solution was concentrated to dryness and dissolved in MeOH (30 mL) at reflux. To the clear solution acetone (30 mL) was added and the mixture was allowed to cool down to ambient temperature to precipitate the product. To the suspension, a second portion of acetone (20 mL) was added and the suspension was aged for an hour. The solid was filtered off and the filter cake was rinsed with acetone (2×30 mL) and dried in the air to afford (2S,5S)-5-(4-chlorobenzyl)-2-methyl-4-(piperidin-4-yl)morpholine dihydrochloride hydrate (4, dihydrochloride hydrate, 12.51 g, 86%% yield over two steps, 98.9% purity by HPLC) as a white solid.

¹H NMR (500 MHz, CD₃OD) δ 7.40-7.30 (m, 4H), 4.08-3.98 (m, 1H), 3.96-3.83 (m, 2H), 3.82-3.74 (m, 1H), 3.69 (d, J=13.3 Hz, 1H), 3.67-3.54 (m, 3H), 3.29-3.06 (m, 5H), 2.60-2.50 (m, 2H), 2.26-2.11 (m, 2H), and 1.32 (d, J=6.2 Hz, 3H) ppm.

¹³C NMR (125 MHz, CD₃OD) δ 135.2, 134.4, 132.5, 130.1, 71.7, 65.7, 58.0, 57.6, 50.4, 43.7, 43.5, 28.4, 25.2, 25.0, and 18.7 ppm.

Example 3 Preparation of methyl (Z)-4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)-N-cyano-piperidine-1-carbimidothioate (6) from (2S,5S)-5-(4-chlorobenzyl)-2-methyl-4-(piperidin-4-yl)morpholine dihydrochloride hydrate (4, dihydrochloride hydrate)

(2S,5S)-5-(4-Chlorobenzyl)-2-methyl-4-(piperidin-4-yl)morpholine dihydrochloride hydrate (4, dihydrochloride hydrate, 5.82 g) and dimethyl N-cyanodithioiminocarbonate (2.34 g) were suspended in ethanol (60 mL). To the suspension, triethylamine (6.1 mL) was added and the reaction mixture was heated up to 40° C. The suspension turned into a clear solution upon heating. After 3 h, the solution was allowed to cool down to ambient temperature and the product precipitated. The suspension was aged and the solid was filtered off. The filter cake was rinsed with ethanol (5 mL) and dried to afford methyl (Z)-4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)-N-cyanopiperidine-1-carbimidothioate (6, 5.48 g, 92% yield, 99.2% purity by HPLC) as a white fluffy solid.

¹H NMR (400 MHz, CDCl₃) δ 7.28-7.22 (m, 2H), 7.13-7.08 (m, 2H), 4.45-4.34 (m, 2H), 3.68-3.54 (m, 2H), 3.46 (dd, J=11.5, 2.7 Hz, 1H), 3.32 (dd, J=12.1, 2.8 Hz, 2H), 3.01 (dd, 0.1=12.9, 10.8 Hz, 1H), 2.88-2.77 (m, 2H), 2.76 (s, 3H), 2.71-2.62 (m, 2H), 2.36 (dd, J=11.8, 10.3 Hz, 1H), 2.07-1.94 (m, 2H), 1.68-1.47 (m, 2H), and 1.21 (d, J=6.2 Hz, 3H) ppm.

¹³C NMR (100 MHz, CDCl₃) δ 168.7, 138.3, 132.0, 130.8, 128.8, 115.4, 72.5, 67.8, 55.8, 55.4, 50.0, 46.9, 30.3, 29.8, 27.5, 19.3, and 16.4 ppm.

FT-IR (ATR): 2959, 2926, 2866, 2820, 2795, 2167, 1541, 1491, 1450, 1431, 1383, 1358, 1273, 1215, 1151, 1117, 1096, 1070, 1043, 1013, 988, 930, 862, 833, 806, 714, 665, and 638 cm⁻¹.

Example 4 Preparation of 4-oxopiperidine methyl N-cyanothioimidocarbamate (14)

Dimethyl N-cyanodithioiminocarbonate (15.02 g) and 4,4-dihydroxypiperidine hydrochloride (19.72 g) were dissolved in a mixture of 2-propanol (60 mL) and water (90 mL). To the solution, triethylamine (17.3 mL) was added. After 2 h the reaction was quenched with 6 M solution of hydrochloric acid (30 mL) and extracted with CH₂Cl₂ (4×75 mL). The combined organic layers were washed with water (75 mL), and 2-propanol (90 mL) was added. The solution was concentrated under atmospheric pressure to volume of 90 mL, then to the boiling solution isopropyl ether (90 mL) was added portionwise, maintaining the reflux. The product precipitated and the suspension was allowed to cool down to ambient temperature. The suspension was aged and the solid was filtered off. The filter cake was rinsed with a mixture of 2-propanol (20 mL) and isopropyl ether (20 mL), and dried to afford 4-oxopiperidine methyl N-cyanothioimidocarbamate (14, 17.94 g, 88% yield) as an off-white solid.

¹H NMR (400 MHz, CDCl₃) δ 4.11 (t, J=6.4 Hz, 4H), 2.85 (s, 3H), 2.60 (t, J=6.3 Hz, 4H) ppm.

¹³C NMR (100 MHz, CDCl₃) δ 204.8, 169.7, 114.5, 46.4, 40.2, 16.4 ppm.

Example 5 Preparation of methyl (Z)-4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)-N-cyano-piperidine-1-carbimidothioate (6) directly from (2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholine (2)

(2S,5S)-5-(4-Chlorobenzyl)-2-methylmorpholine (2, 5.23 g), 4-oxopiperidine methyl N-cyanothioimidocarbamate (14, 6.86 g) and zinc chloride (3.16 g) were suspended in ethanol (52 mL). The slightly cloudy solution was cooled down to 0° C. and sodium cyanoborohydride (2.19 g) was added portionwise. The suspension was stirred at ambient temperature for 24 h. The reaction was quenched by addition of 1 M solution of sodium hydroxide (60 mL) and extracted with dichloromethane (60 mL, then 2×30 mL). The combined organic layers were washed with water (30 mL) and the solvent was swapped to ethanol. During the swap the product precipitated. The suspension was allowed to cool down to ambient temperature and the solid was filtered off. The filter cake was rinsed with ethanol (18 mL) and dried to afford methyl (Z)-4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)-N-cyanopiperidine-1-carbimidothioate (6, 7.80 g, 83% yield, 99.5% purity by HPLC) as an off-white solid.

¹H NMR (400 MHz, CDCl₃) δ 7.28-7.22 (m, 2H), 7.13-7.08 (m, 2H), 4.45-4.34 (m, 2H), 3.68-3.54 (m, 2H), 3.46 (dd, J=11.5, 2.7 Hz, 1H), 3.32 (dd, J=12.1, 2.8 Hz, 2H), 3.01 (dd, 0.1=12.9, 10.8 Hz, 1H), 2.88-2.77 (m, 2H), 2.76 (s, 3H), 2.71-2.62 (m, 2H), 2.36 (dd, J=11.8, 10.3 Hz, 1H), 2.07-1.94 (m, 2H), 1.68-1.47 (m, 2H), and 1.21 (d, J=6.2 Hz, 3H) ppm.

¹³C NMR (100 MHz, CDCl₃) δ 168.7, 138.3, 132.0, 130.8, 128.8, 115.4, 72.5, 67.8, 55.8, 55.4, 50.0, 46.9, 30.3, 29.8, 27.5, 19.3, and 16.4 ppm.

FT-IR (ATR): 2959, 2926, 2866, 2820, 2795, 2167, 1541, 1491, 1450, 1431, 1383, 1358, 1273, 1215, 1151, 1117, 1096, 1070, 1043, 1013, 988, 930, 862, 833, 806, 714, 665, and 638 cm⁻¹.

Example 6 Preparation of 5-(4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)piperidin-1-yl)-4H-1,2,4-triazol-3-amine hydrated form I (1, hydrated form I) from (2S,5S)-5-(4-chlorobenzyl)-2-methyl-4-(piperidin-4-yl)morpholine dihydrochloride hydrate (4, dihydrochloride hydrate)

(2S,5S)-5-(4-Chlorobenzyl)-2-methyl-4-(piperidin-4-yl)morpholine dihydrochloride hydrate (4, dihydrochloride hydrate, 9.03 g) and dimethyl N-cyanodithioiminocarbonate (3.80 g) were suspended in 1-propanol (72 mL). Triethylamine (9.9 mL) was added and the clear solution was refluxed for 3 hours. Hydrazine monohydrate (3.5 mL) was added and the reaction was further carried out at 60° C. for additional 2 hours. Water (144 mL) was added to the hot solution that was allowed to cool down to ambient temperature, seeded with a crystalline material and put into a refrigerator for 24 hours. The precipitate was filtered off and the filter cake was rinsed with water (2×40 mL) and dried in the air to afford crude product (14.3 g) as 5-(4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)piperidin-1-yl)-4H-1,2,4-triazol-3-amine hydrated form I (1, hydrated form I, 7.06 g, 25% loss on drying, 80% yield on dry basis, 99.4% purity by HPLC) as a white solid.

The seed crystalline material used was obtained from the crude reaction mixture. The reaction mixture was concentrated to dryness under reduced pressure and the residue was purified by chromatography on silica (EtOAc:MeOH 1:0→200:1→100:1→50:1→20:1→10:1). The fractions containing the product were combined and concentrated to dryness under reduced pressure. The residue was dissolved in acetonitrile (10 mL/1 g of the product) at reflux. The solution was allowed to cool down to ambient temperature to precipitate the product. The solid was filtered off and rinsed with acetonitrile to afford the seed.

¹H NMR (500 MHz, CD₃OD) δ 7.29-7.25 (m, 2H), 7.21-7.16 (m, 2H), 3.67-3.54 (m, 2H), 3.47 (d, J=11.5 Hz, 1H), 3.01-2.72 (m, 6H), 2.72-2.63 (m, 1H), 2.35 (dd, J=12.0, 10.5 Hz, 1H), 2.10-1.95 (m, 2H), 1.58-1.39 (m, 2H), and 1.19 (d, J=6.2 Hz, 3H) ppm.

¹³C NMR (125 MHz, CD₃OD) δ 140.1, 132.9, 132.0, 129.6, 73.7, 68.5, 57.6, 56.7, 50.9, 46.7, 30.4, 29.9, 28.1, and 19.4 ppm.

FT-IR (ATR): 3318, 3206, 2963, 2934, 2859, 2833, 1636, 1589, 1553, 1489, 1462, 1404, 1346, 1314, 1277, 1250, 1151, 117, 1092, 1069, 1013, 917, 868, 829, 800, 764, 725, and 673 cm⁻¹.

Example 7 Preparation of 5-(4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)piperidin-1-yl)-4H-1,2,4-triazol-3-amine hydrated form I (1, hydrated form I) from methyl (Z)-4-((2S,5S)-5-(4-chloro-benzyl)-2-methylmorpholino)-N-cyanopiperidine-1-carbimidothioate (6)

Methyl (Z)-4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)-N-cyanopiperidine-1-carbimidothioate (6, 7.51 g) was suspended in ethanol (37 mL) and hydrazine hydrate (2.67 mL) was added. The suspension was heated up to 60° C. and a clear solution was obtained. After 2 h water (113 mL) was added and the product precipitated upon cooling to ambient temperature. The solid was filtered off and the filter cake was rinsed with water (37 mL), and dried to afford 5-(4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)piperidin-1-yl)-4H-1,2,4-triazol-3-amine hydrated form I (1, hydrated form I, 15.82 g, 36% loss on drying, 133% yield, 99.7% purity by HPLC) as a white solid.

¹H NMR (500 MHz, CD₃OD) δ 7.29-7.25 (m, 2H), 7.21-7.16 (m, 2H), 3.67-3.54 (m, 2H), 3.47 (d, J=11.5 Hz, 1H), 3.01-2.72 (m, 6H), 2.72-2.63 (m, 1H), 2.35 (dd, J=12.0, 10.5 Hz, 1H), 2.10-1.95 (m, 2H), 1.58-1.39 (m, 2H), and 1.19 (d, J=6.2 Hz, 3H) ppm.

¹³C NMR (125 MHz, CD₃OD) δ 140.1, 132.9, 132.0, 129.6, 73.7, 68.5, 57.6, 56.7, 50.9, 46.7, 30.4, 29.9, 28.1, and 19.4 ppm.

FT-IR (ATR): 3318, 3206, 2963, 2934, 2859, 2833, 1636, 1589, 1553, 1489, 1462, 1404, 1346, 1314, 1277, 1250, 1151, 117, 1092, 1069, 1013, 917, 868, 829, 800, 764, 725, and 673

Example 8 Preparation of 5-(4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)piperidin-1-yl)-4H-1,2,4-triazol-3-amine anhydrous form (1, anhydrous form) from 5-(4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)piperidin-1-yl)-4H-1,2,4-triazol-3-amine hydrated form I (1, hydrated form I)

5-(4-((2S,5S)-5-(4-Chlorobenzyl)-2-methyl morpholino)piperidin-1-yl)-4H-1,2,4-triazol-3-amine hydrated form I (1, hydrated form I, 6.62 g calculated on dry basis) was suspended in ethyl acetate (66 mL) and the suspension was heated up to reflux. Upon heating, the suspension turned into a clear solution. Water was distilled off using a Dean-Stark trap until boiling point of 76° C. was reached. During the distillation the product precipitated. The suspension was allowed to cool down to ambient temperature and the solid was filtered off. The filter cake was rinsed with ethyl acetate (13 mL) and dried to afford 5-(4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)piperidin-1-yl)-4H-1,2,4-triazol-3-amine anhydrous form (1, anhydrous form, 6.38 g, 83% yield, >99.9% purity by HPLC) as white crystals.

¹H NMR (700 MHz, C₆D₆/CD₃OD) δ 7.13 (d, J=8.2 Hz, 2H), 6.89 (d, J=8.2 Hz, 2H), 3.99 (br s, 2H), 3.66 (br s, 3H), 3.56 (d, J=11.4 Hz, 1H), 3.54-3.46 (m, 1H), 3.37 (d, J=11.4 Hz, 1H), 2.90-2.80 (m, 3H), 2.68 (d, J=10.4 Hz, 1H), 2.40 (d, J=11.9 Hz, 2H), 2.32-2.25 (m, 1H), 2.05 (t, J=11.2 Hz, 1H), 1.81 (d, J=12.5 Hz, 1H), 1.65 (d, J=12.5 Hz, 1H), 1.54-1.46 (m, 1H), 1.46-1.37 (m, 1H), and 1.11 (d, J=6.2 Hz, 3H) ppm.

¹³C NMR (175 MHz, C₆D₆) δ 139.0, 132.1, 131.2, 129.0, 128.1, 72.6, 67.8, 56.5, 55.7, 50.1, 48.9, 45.8, 45.7, 29.7, 29.2, 27.7, and 19.3 ppm.

FT-IR (ATR): 3252, 3198, 3119, 2955, 2924, 2857, 2793, 1666, 1599, 1543, 1483, 1456, 1404, 1337, 1283, 1248, 1136, 1117, 1094, 1072, 1053, 1013, 908, 858, 795, and 718 cm⁻¹.

Example 9 Preparation of 5-(4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)piperidin-1-yl)-4H-1,2,4-triazol-3-amine anhydrous form (1, anhydrous form) from methyl (Z)-4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)-N-cyanopiperidine-1-carbimidothioate (6)

Methyl (Z)-4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)-N-cyanopiperidine-1-carbimidothioate (6, 5.05 g) was suspended in acetonitrile (50 mL) and hydrazine hydrate (1.78 mL) was added. The suspension was heated up to 60° C. and clear solution was obtained. After 2 h, the solution was allowed to cool down to ambient temperature and the product precipitated. The solid was filtered off, and the filter cake was rinsed with acetonitrile (12.5 mL) to afford 5-(4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)piperidin-1-yl)-4H-1,2,4-triazol-3-amine anhydrous form (1, anhydrous form, 4.39 g, 90% yield, 98.7% purity by HPLC) as white crystals.

¹H NMR (700 MHz, C₆D₆/CD₃OD) δ 7.13 (d, J=8.2 Hz, 2H), 6.89 (d, J=8.2 Hz, 2H), 3.99 (br s, 2H), 3.66 (br s, 3H), 3.56 (d, J=11.4 Hz, 1H), 3.54-3.46 (m, 1H), 3.37 (d, J=11.4 Hz, 1H), 2.90-2.80 (m, 3H), 2.68 (d, J=10.4 Hz, 1H), 2.40 (d, J=11.9 Hz, 2H), 2.32-2.25 (m, 1H), 2.05 (t, J=11.2 Hz, 1H), 1.81 (d, J=12.5 Hz, 1H), 1.65 (d, J=12.5 Hz, 1H), 1.54-1.46 (m, 1H), 1.46-1.37 (m, 1H), and 1.11 (d, J=6.2 Hz, 3H) ppm.

¹³C NMR (175 MHz, C₆D₆) δ 139.0, 132.1, 131.2, 129.0, 128.1, 72.6, 67.8, 56.5, 55.7, 50.1, 48.9, 45.8, 45.7, 29.7, 29.2, 27.7, and 19.3 ppm.

FT-IR (ATR): 3252, 3198, 3119, 2955, 2924, 2857, 2793, 1666, 1599, 1543, 1483, 1456, 1404, 1337, 1283, 1248, 1136, 1117, 1094, 1072, 1053, 1013, 908, 858, 795, and 718 cm⁻¹.

Example 10 Preparation of 5-(4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)piperidin-1-yl)-4H-1,2,4-triazol-3-amine hydrated form II (1, hydrated form II) from 5-(4-((2S,5S)-5-(4-chlorobenzyl)-2-methyl morpholino)piperidin-1-yl)-4H-1,2,4-triazol-3-amine anhydrous form (1, anhydrous form)

5-(4-((2S,5S)-5-(4-Chlorobenzyl)-2-methyl morpholino)piperidin-1-yl)-4H-1,2,4-triazol-3-amine anhydrous form (1, anhydrous form, 5.03 g) was dissolved in methanol (20 mL) at reflux. Water (30 mL) was slowly added maintaining the reflux. Upon addition the product precipitated. The suspension was allowed to cool down to ambient temperature and was aged for an hour. The solid was filtered off and the filter cake was rinsed with a mixture of methanol and water (25 mL, 2:3 vol./vol.), and dried in the air overnight to afford 5-(4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)piperidin-1-yl)-4H-1,2,4-triazol-3-amine hydrated form II (1, hydrated form II, 5.44 g, 8.2% water by Karl-Fischer, 99% yield on dry basis, >99.9% purity by HPLC) as a white solid.

Example 11 Preparation of 5-(4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)piperidin-1-yl)-4H-1,2,4-triazol-3-amine amorphous form (1, amorphous form) from 5-(4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)piperidin-1-yl)-4H-1,2,4-triazol-3-amine anhydrous form (1, anhydrous form)

A Petri dish covered with 5-(4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)piperidin-1-yl)-4H-1,2,4-triazol-3-amine anhydrous form (1, anhydrous form, 5.02 g) was placed on a hot-plate heated up to 200° C. When the material melted, the dish was allowed to cool down to ambient temperature. The glass-like material was ground in a mortar to afford 5-(4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)piperidin-1-yl)-4H-1,2,4-triazol-3-amine amorphous form (1, amorphous form, 4.82 g, 96% yield, >99.9% purity by HPLC) as a white solid.

¹H NMR (700 MHz, C₆D₆/CD₃OD) δ 7.13 (d, J=8.2 Hz, 2H), 6.89 (d, J=8.2 Hz, 2H), 3.99 (br s, 2H), 3.66 (br s, 3H), 3.56 (d, J=11.4 Hz, 1H), 3.54-3.46 (m, 1H), 3.37 (d, J=11.4 Hz, 1H), 2.90-2.80 (m, 3H), 2.68 (d, J=10.4 Hz, 1H), 2.40 (d, J=11.9 Hz, 2H), 2.32-2.25 (m, 1H), 2.05 (t, J=11.2 Hz, 1H), 1.81 (d, J=12.5 Hz, 1H), 1.65 (d, J=12.5 Hz, 1H), 1.54-1.46 (m, 1H), 1.46-1.37 (m, 1H), and 1.11 (d, J=6.2 Hz, 3H) ppm.

¹³C NMR (175 MHz, C₆D₆) δ 139.0, 132.1, 131.2, 129.0, 128.1, 72.6, 67.8, 56.5, 55.7, 50.1, 48.9, 45.8, 45.7, 29.7, 29.2, 27.7, and 19.3 ppm.

FT-IR (ATR): 3312, 3173, 2968, 2859, 2822, 1634, 1551, 1489, 1458, 1346, 1277, 1246, 1150, 1115, 1094, 1069, 1013, 920, 858, 804, 758, 719, and 665 cm⁻¹.

Example 12 Preparation of 5-(4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)piperidin-1-yl)-4H-1,2,4-triazol-3-amine amorphous form (1, amorphous form) from 5-(4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)piperidin-1-yl)-4H-1,2,4-triazol-3-amine hydrated form I or II (1, hydrated form I or II)

A Petri dish covered with 5-(4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)piperidin-1-yl)-4H-1,2,4-triazol-3-amine hydrated form I or II (1, hydrated form I or II, 5.01 g) was placed on a hot-plate heated up to 125° C. When the material melted, the dish was allowed to cool down to ambient temperature. The glass-like material was ground in a mortar to afford 5-(4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)piperidin-1-yl)-4H-1,2,4-triazol-3-amine amorphous form (1, amorphous form, 4.49 g, 90% yield, >99.99% purity by HPLC starting from hydrated form I, and 1, amorphous form, 4.41 g, 88% yield, >99.9% purity by HPLC starting from hydrated form II) as a white solid.

¹H NMR (700 MHz, C₆D₆/CD₃OD) δ 7.13 (d, J=8.2 Hz, 2H), 6.89 (d, J=8.2 Hz, 2H), 3.99 (br s, 2H), 3.66 (br s, 3H), 3.56 (d, J=11.4 Hz, 1H), 3.54-3.46 (m, 1H), 3.37 (d, J=11.4 Hz, 1H), 2.90-2.80 (m, 3H), 2.68 (d, J=10.4 Hz, 1H), 2.40 (d, J=11.9 Hz, 2H), 2.32-2.25 (m, 1H), 2.05 (t, J=11.2 Hz, 1H), 1.81 (d, J=12.5 Hz, 1H), 1.65 (d, J=12.5 Hz, 1H), 1.54-1.46 (m, 1H), 1.46-1.37 (m, 1H), and 1.11 (d, J=6.2 Hz, 3H) ppm.

¹³C NMR (175 MHz, C₆D₆) δ 139.0, 132.1, 131.2, 129.0, 128.1, 72.6, 67.8, 56.5, 55.7, 50.1, 48.9, 45.8, 45.7, 29.7, 29.2, 27.7, and 19.3 ppm.

FT-IR (ATR): 3312, 3173, 2968, 2859, 2822, 1634, 1551, 1489, 1458, 1346, 1277, 1246, 1150, 1115, 1094, 1069, 1013, 920, 858, 804, 758, 719, and 665 cm⁻¹. 

1. A process for the preparation of (2S,5S)-5-(4-chlorobenzyl)-2-methyl-4-(piperidin-4-yl)morpholine of formula 5

the process comprising: a) reacting (2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholine of formula 2

with N-Boc-4-piperidinone of formula 3

and sodium cyanoborohydride in an alcohol as a solvent, to provide tert-butyl 4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)piperidine-1-carboxylate of formula 4

b) removal of tert-butoxycarbonyl protecting group using hydrochloric acid to provide (2S,5S)-5-(4-chlorobenzyl)-2-methyl-4-(piperidin-4-yl)morpholine of formula
 5. 2. The process of claim 1, wherein in step (a) the compound of formula 2 is used as its hydrochloride salt, and/or wherein in step (a) zinc chloride is added; and/or wherein in step (a) methanol is used as a solvent and/or wherein in step (b) ethyl acetate is used as a solvent. 3-5. (canceled)
 6. A solid crystalline form of (Z)-4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)-N-cyanopiperidine-1-carbimidothioate of formula 6

characterized by: a) an XRPD pattern comprising at least the following peaks: 12.03±0.1, 20.18±0.1, 22.56±0.1, and 24.08±0.1° 2-theta; b) characteristic infrared (IR) spectrum comprising IR bands at 2959, 2926, 2866, 2820, 2795, 2167, 1541, 1491, 1450, 1431, 1383, 1358, 1273, 1215, 1151, 1117, 1096, 1070, 1043, 1013, 988, 930, 862, 833, 806, 714, 665, and 638 cm⁻¹; and c) DSC thermogram, with onset at 156.26° C.±2.0° C. and a peak at 157.51° C.±2.0° C.
 7. A solid crystalline form of 5-(4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpho-lino)piperidin-1-yl)-1H-1,2,4-triazol-3-amine of formula 1

hydrated form I, characterized by: a) an XRPD pattern comprising at least the following peaks: 14.20±0.1, 15.58±0.1, 18.30±0.1, 23.22±0.1, and 23.68±0.1° 2-theta; and b) characteristic infrared (IR) spectrum comprising IR bands at 3318, 3206, 2963, 2934, 2859, 2833, 1636, 1589, 1553, 1489, 1462, 1404, 1346, 1314, 1277, 1250, 1151, 117, 1092, 1069, 1013, 917, 868, 829, 800, 764, 725, and 673 cm⁻¹.
 8. A solid crystalline form of 5-(4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)piperidin-1-yl)-1H-1,2,4-triazol-3-amine anhydrous form, characterized by: a. an XRPD pattern comprising at least the following peaks: 14.61±0.1, 19.86±0.1, and 21.22±0.1° 2-theta; b. characteristic infrared (IR) spectrum comprising IR bands at 3252, 3198, 3119, 2955, 2924, 2857, 2793, 1666, 1599, 1543, 1483, 1456, 1404, 1337, 1283, 1248, 1136, 1117, 1094, 1072, 1053, 1013, 908, 858, 795, and 718 cm⁻¹; and c. DSC thermogram, with onset at 175.83° C.±2.0° C. and a peak at 177.59° C.±2.0° C.
 9. A process for the preparation of 5-(4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)piperidin-1-yl)-1H-1,2,4-triazol-3-amine of formula 1, comprising: a) reaction of the compound of formula 5 with dimethyl N-cyanodithioiminocarbonate in the presence of a base in a solvent, leading to (Z)-4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)-N-cyanopiperidine-1-carbimidothioate of formula 6; and b) reaction of the compound of formula 6 with hydrazine monohydrate in a solvent, to provide the compound of formula
 1. 10. The process of claim 9, wherein in step (a) the compound of formula 5 is in a salt form, and/or wherein in step (a) the base is a trialkylamine; and/or wherein in step (a) ethanol, 1-propanol or 2-propanol or acetonitrile is used as a solvent. 11-15. (canceled)
 16. The process of claim 10, wherein in step (a) the solvent is ethanol, 1-propanol or 2-propanol, and wherein the compound of formula 6 is isolated after step (a) by precipitation upon cooling of the reaction mixture.
 17. The process of claim 10, wherein in step (a) the solvent is ethanol, 1-propanol or 2-propanol, and wherein step (b) is performed without isolation of the compound of formula
 6. 18. The process of claim 10, wherein in step (a) the solvent is ethanol, 1-propanol or 2-propanol, and wherein the compound of formula 1 is isolated after step (b) by precipitation upon addition of water to the reaction mixture.
 19. The process of claim 17, wherein the compound of formula 1 is isolated after step (b) by precipitation upon addition of water to the reaction mixture.
 20. The process of claim 15, 10, wherein in step (a) the solvent is acetonitrile, and wherein the compound of formula 1 is isolated after step (b) by precipitation upon cooling of the reaction mixture.
 21. A process for the preparation of 4-oxopiperidine methyl N-cyanothioimidocarbamate of formula 14

comprising reacting dimethyl N-cyanodithioiminocarbonate, 4,4-dihydroxypiperidine hydrochloride and a base in a solvent.
 22. The process of claim 21, wherein the base is a trialkylamine, and/or wherein the solvent is a mixture of water and 2-propanol; and/or wherein the product of formula 14 is purified by crystallization. 23-26. (canceled)
 27. A process for the preparation of the compound of formula 6, comprising reacting the compound of formula 2 and the compound of formula 14 and sodium cyanoborohydride and an inorganic salt in a solvent.
 28. The process of claim 27, wherein the solvent is ethanol; and/or wherein zinc chloride is used as an additive; and/or wherein the product of formula 6 is purified by crystallization; and/or wherein the compound of formula 2 is used in a salt form. 29-32. (canceled)
 33. A process for the preparation of anhydrous form of 5-(4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)piperidin-1-yl)-1H-1,2,4-triazol-3-amine of formula 1 comprising azeotropic distillation of a solution of the starting compound of formula 1 hydrated form I or II.
 34. The process of claim 33, wherein the starting compound of formula 1 is the hydrated form I.
 35. A solid crystalline form of 5-(4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpho-lino)piperidin-1-yl)-1H-1,2,4-triazol-3-amine of formula 1 hydrated form II, characterized by a) an XRPD pattern comprising at least the following peaks: 15.48±0.1, 19.76±0.1, 22.54±0.1, and 22.86±0.1° 2-theta; and b) characteristic infrared (IR) spectrum comprising IR bands at 3325, 2963, 2814, 1634, 1580, 1553, 1489, 1460, 1418, 1389, 1343, 1279, 1248, 1206, 1151, 1119, 1090, 1069, 1047, 1013, 991, 914, 866, 831, 797, 760, 665, and 600 cm⁻¹.
 36. A process for the preparation of the hydrated form II of 5-(4-((2S,5S)-5-(4-chloro-benzyl)-2-methylmorpholino)piperidin-1-yl)-1H-1,2,4-triazol-3-amine of formula 1 comprising crystallization of anhydrous form of the compound of formula 1 from a mixture of methanol and water.
 37. A solid amorphous form of 5-(4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)piperidin-1-yl)-1H-1,2,4-triazol-3-amine of formula 1, characterized by characteristic infrared (IR) spectrum comprising IR bands at 3312, 3173, 2968, 2859, 2822, 1634, 1551, 1489, 1458, 1346, 1277, 1246, 1150, 1115, 1094, 1069, 1013, 920, 858, 804, 758, 719, and 665 cm⁻¹.
 38. A process for the preparation of amorphous form of 5-(4-((2S,5S)-5-(4-chlorobenzyl)-2-methylmorpholino)piperidin-1-yl)-1H-1,2,4-triazol-3-amine of formula 1 by melting the starting compound of formula 1 either in anhydrous form or in hydrated form I or II.
 39. The process of claim 38, wherein the starting compound of formula 1 is the anhydrous form and the temperature of melting is 200° C., or wherein the starting compound of formula 1 is the hydrated form I and the temperature of melting is 125° C.
 40. (canceled) 